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Autosomal Recessive Nonsyndromic Deafness 113
An autosomal recessive nonsyndromic deafness characterized by postlingual progressive hearing impairment that is caused by homozygous or compound heterozygous mutation in the CEACAM16 gene on chromosome 19q13.
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Overview
An autosomal recessive nonsyndromic deafness characterized by postlingual progressive hearing impairment that is caused by homozygous or compound heterozygous mutation in the CEACAM16 gene on chromosome 19q13.
Resources
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